A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18163145



Internal ID20730185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116439874..116442182hg38UCSC Ensembl
chr8:117452112..117454420hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg382309
hg192309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424442
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18163145
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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